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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400356Generated: November 1, 2026

Glyoxal → 7-[1,2,4]Triazin-3-yl-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/2400356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantGlyoxalHCID 7860—
ReactantHCID 178512584HCID 178512584—
SolventEthanolHCID 702—
Product7-[1,2,4]Triazin-3-yl-imidazo[1,2-a]pyridineHCID 6898422880%

Reaction Steps

To half the material from step d (ca. 2.3 mmol) was added glyoxal (40% in water, 1 ml) and ethanol (15 ml) and the mixture heated to 100 deg C. After 1 hour the reaction was allowed to cool and was concentrated in vacuo. Water and dichloromethane was added and the mixture filtered under suction. The organic liquors were discarded and the aqueous layer was basified with 2N sodium hydroxide solution. To this was added dichloromethane and the mixture was again filtered under suction. The dichloromethane layer was separated and concentrated to furnish 289 mg of a yellow solid (80% clean). MS: [M+H]+198

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796244B2
Source datasetuspto-grants-2014_08
ORD IDord-2367ad7f05f946268ed91ae7f1029057
Source noteuspto-grants-2014_08